Abstract

Objective. Olanzapine is proved to be effective for chemotherapy induced nausea and vomiting (CINV). But its efficacy in combination with standard antiemetic therapy is unknown. The purpose of this study is to prove the preventive effect of olanzapine for the prevention of CINV caused by highly emetogenic chemotherapy when used with standard antiemetic therapy. Method. Gynecologic cancer patients receiving cisplatin-based chemotherapy who had grade 2 or 3 nausea in overall phase (0–120 h after chemotherapy) despite standard therapy were assigned to this study. From the next cycles to cycles in which patients developed grade 2 or 3 nausea, they received olanzapine with standard therapy. 5 mg oral olanzapine was administered for 7 days from the day before chemotherapy. The effectiveness of preventive administration of olanzapine was evaluated retrospectively. The primary endpoint was nausea control rate (grade 0 or 1) with olanzapine. Results. Fifty patients were evaluable. The nausea control rate with olanzapine was improved from 58% to 98% in acute phase (0–24 h after chemotherapy) and 2% to 94% in delayed phase (24–120 h after chemotherapy). In overall phase, the nausea control rate improved from 0% to 92%, and it was statistically significant (P < 0.001). Conclusion. Preventive use of olanzapine combined with standard antiemetic therapy showed improvement in control of refractory nausea.

Highlights

  • Chemotherapy induced nausea and vomiting (CINV) is one of the most harmful adverse effects even though there is a significant progress in antiemetics nowadays

  • National Comprehensive Cancer Network (NCCN), American Society of Clinical Oncology (ASCO), and Multinational Association of Supportive Care in Cancer (MASCC) have developed antiemetic guidelines based on evidence

  • These guidelines recommend triple therapy consisted of 5-HT3 receptor antagonist, NK-1 receptor antagonist, and dexamethasone as a standard antiemetic therapy toward highly emetogenic chemotherapy (HEC) [1, 2]

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Summary

Introduction

Chemotherapy induced nausea and vomiting (CINV) is one of the most harmful adverse effects even though there is a significant progress in antiemetics nowadays. In Japan, the first guideline for proper use of antiemetics was provided by Japan Society of Clinical Oncology in 2010 based on guidelines written above. These guidelines recommend triple therapy consisted of 5-HT3 receptor antagonist, NK-1 receptor antagonist, and dexamethasone as a standard antiemetic therapy toward highly emetogenic chemotherapy (HEC) [1, 2]. There is no effective therapy toward CINV which is resistant to standard antiemetics reported

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